Inherited cancer-predisposing syndrome
Institutions de rang supérieur 0
Conseil génétique 2
Humangenetisches Institut am Universitätsklinikum Erlangen
Universitätsklinikum Erlangen
                    Schwabachanlage 10
                    91054 Erlangen
                
                             09131 8522318
                            
 09131 8523232
                            
                                
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- Li-Fraumeni syndrome
 - Beckwith-Wiedemann syndrome
 - Diamond-Blackfan anemia
 - Inherited cancer-predisposing syndrome
 - Constitutional mismatch repair deficiency syndrome
 - Von Hippel-Lindau disease
 - Noonan syndrome
 - Ataxia-telangiectasia
 - Hereditary nonpolyposis colon cancer
 - Familial ovarian cancer
 - Full NF2-related schwannomatosis
 - Hereditary retinoblastoma
 - Silver-Russell syndrome
 - Common variable immunodeficiency
 - Xeroderma pigmentosum
 
Institut für Humangenetik am Universitätsklinikum Hamburg-Eppendorf
Universitätsklinikum Hamburg-Eppendorf (UKE)
                    Martinistraße 52
                    20251 Hamburg
                
                             040 741053125
                            
 040 741055138
                            
                                
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- Inherited renal cancer-predisposing syndrome
 - Noonan syndrome
 - Li-Fraumeni syndrome
 - Diamond-Blackfan anemia
 - Familial ovarian cancer
 - Full NF2-related schwannomatosis
 - APC-related attenuated familial adenomatous polyposis
 - Costello syndrome
 - Von Hippel-Lindau disease
 - Ataxia-telangiectasia
 - Silver-Russell syndrome
 - Cockayne syndrome
 - Xeroderma pigmentosum
 - Maffucci syndrome
 - Beckwith-Wiedemann syndrome
 
Institutions de prise en charge 4
Zentrum für seltene Lebererkrankungen und gastrointestinale Erkrankungen der Uniklinik RWTH Aachen
Zentrum für Seltene Erkrankungen Aachen Uniklinik RWTH Aachen
                    Pauwelsstr. 30
                    52074 Aachen
                
- HJV or HAMP-related hemochromatosis
 - Primary biliary cholangitis
 - Porphyria
 - Hereditary chronic pancreatitis
 - Congenital erythropoietic porphyria
 - Budd-Chiari syndrome
 - Familial adenomatous polyposis
 - TFR2-related hemochromatosis
 - Peutz-Jeghers syndrome
 - VIPoma
 - Alpha-1-antitrypsin deficiency
 - Cholangiocarcinoma
 - Primary sclerosing cholangitis
 - Fabry disease
 - Wilson disease
 
Zentrum für seltene hämatologische Erkrankungen der Uniklinik RWTH Aachen
Uniklinik RWTH Aachen Zentrum für Seltene Erkrankungen Aachen
                    Pauwelsstr. 30
                    52074 Aachen
                
- Dyskeratosis congenita
 - Essential thrombocythemia
 - Chronic myeloproliferative disease, unclassifiable
 - Idiopathic aplastic anemia
 - Autosomal dominant aplasia and myelodysplasia
 - Mast cell leukemia
 - Classic mast cell leukemia
 - Hereditary isolated aplastic anemia
 - Paroxysmal nocturnal hemoglobinuria
 - Myelodysplastic syndrome
 - Aggressive systemic mastocytosis
 - Mastocytosis
 - Myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality
 - Chronic eosinophilic leukemia
 - Chronic myeloid leukemia
 
Zentrum für Tumordispositionssyndrome (ZeKiTDS) am Universitätsklinikum Augsburg
Augsburger Zentrum für Seltene Erkrankungen (AZeSE)
                    Stenglinstraße 2
                    86156 Augsburg
                
                             0821 4009300
                            
 0821 400179330
                            
                                
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Zentrum für Menschen mit Hämoglobinopathien am Universitätsklinikum Essen
Universitätsklinikum Essen Essener Zentrum für Seltene Erkrankungen (EZSE)
                    Hufelandstr. 55
                    45147 Essen